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Nektar Announces Publication In Blood Of Phase 1 Data For Novel IL-15 Agonist NKTR-255 In Combination With Autologous CD19-22 CAR-T Cell Therapy In Patients With B-cell Acute Lymphoblastic Leukemia

Nektar Announces Publication In Blood Of Phase 1 Data For Novel IL-15 Agonist NKTR-255 In Combination With Autologous CD19-22 CAR-T Cell Therapy In Patients With B-cell Acute Lymphoblastic Leukemia

Nektar宣佈在《血液》雜誌上公佈了關於新型IL-15激動劑NKTR-255與自體CD19-22 CAR-t細胞治療聯合應用的一期數據,用於治療b細胞急性淋巴細胞白血病患者
Benzinga ·  10/18 00:10

– Relapse-free/progression-free survival for NKTR-255 plus CD19-22 CAR-T cell therapy at 12 months was double that of historical controls (67% vs 38%) –

– 在12個月時,NKTR-255聯合CD19-22 CAR-T細胞治療的無復發/無進展生存率是歷史對照的兩倍(67% vs 38%)–

– Eight of nine patients achieved complete remission, all without detectable MRD –

– 九名患者中有八名達到完全緩解,均無可檢測的MRD–

SAN FRANCISCO, Oct. 17, 2024 /PRNewswire/ -- Nektar Therapeutics (NASDAQ:NKTR) today announced the publication of the first clinical data from a Phase 1 study evaluating NKTR-255 in combination with an autologous bispecific chimeric antigen receptor (CAR)-T cell therapy targeting CD19 and CD22 in patients with relapsed or refractory B-cell acute lymphoblastic leukemia (B-ALL) in Blood, the peer-reviewed medical journal of the American Society of Hematology.

舊金山,2024年10月17日 / PRNewswire / - 內克塔治療(納斯達克:NKTR)今天宣佈了第一項評估NKTR-255與自體雙特異性嵌合抗原受體(CAR-T)細胞治療結合治療CD19和CD22的復發或難治性B細胞急性淋巴細胞白血病(b-ALL)患者的1期研究臨床數據刊登在美國血液學會同行評議醫學期刊Blood中。

NKTR-255 is a novel IL-15 receptor agonist currently being studied in clinical trials in combination with cellular therapies and immune checkpoint inhibitors. NKTR-255 has shown in previous clinical studies that it can proliferate a range of immune cells and augment lymphocyte trafficking.1,2

NKTR-255是一種新型IL-15受體激動劑,目前正在臨床試驗中研究,結合細胞療法和免疫檢查點抑制劑。 就以往的臨床研究顯示,NKTR-255可以擴增一系列免疫細胞並增強淋巴細胞的轉運。1,2

The data published in Blood showed favorable efficacy with eight out of nine patients (89%) whom successfully received CAR19-22 followed by NKTR-255 achieving measurable residual disease (MRD) negative remission. The study further demonstrated that, at 12 months, relapse-free/progression-free survival for NKTR-255 in combination with the CD19-22 CAR-T cell therapy was double that of historical controls (67% vs 38%).

在Blood雜誌中公佈的數據顯示,成功接受CAR19-22後接受NKTR-255治療的九名患者中有八名(89%)實現了可測量殘餘疾病(MRD)陰性緩解。該研究進一步表明,12個月時,NKTR-255聯合CD19-22 CAR-T細胞療法的無復發/無進展生存率是歷史對照的兩倍(67% vs 38%)。

譯文內容由第三人軟體翻譯。


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